Sen Aritro, Bettegowda Anilkumar, Jimenez-Krassel Fermin, Ireland James J, Smith George W
Laboratory of Mammalian Reproductive Biology and Genomics, Department of Animal Science, Michigan State University, 1230 Anthony Hall, East Lansing, Michigan 48824, USA.
Endocrinology. 2007 Sep;148(9):4400-10. doi: 10.1210/en.2007-0332. Epub 2007 Jun 14.
Regulation of estradiol production, central to ovarian follicular development and reproductive function, is mediated by a complex interaction of pituitary gonadotropins such as FSH with locally produced regulatory molecules. We previously demonstrated a negative association of expression of cocaine-and amphetamine-regulated transcript (CART) with follicle health status and a novel local negative role for CART in regulation of basal estradiol production by bovine granulosa cells. However, effects of CART on FSH-induced estradiol production and the underlying mechanism(s) mediating the physiological actions of CART on granulosa cells are not known. Objectives of the present study were to determine effects of CART on basal and FSH-induced intracellular cAMP levels, aromatase mRNA, estradiol accumulation, calcium signaling, and the intracellular signaling pathways involved using primary cultures of bovine granulosa cells. CART treatment potently inhibits the FSH-induced rise in granulosa cell cAMP levels, estradiol accumulation, and aromatase mRNA. Furthermore, results show that calcium is essential for FSH-induced cAMP and estradiol accumulation, and CART significantly inhibits FSH-induced calcium influx. Select G protein and protein kinase inhibitors were used to elucidate pathways involved in CART actions. The inhibitory actions of CART on FSH signaling and estradiol production are mediated via a G(o/i)-dependent pathway, whereas none of the other signaling inhibitors had any effect on CART actions. Results demonstrate novel potent inhibitory effects of CART on multiple components of the FSH signaling pathway linked to estradiol production and follicular development and shed new insight into the mechanism of action of CART potentially pertinent within and beyond the reproductive system.
雌二醇的产生调控是卵巢卵泡发育和生殖功能的核心,它由垂体促性腺激素(如促卵泡激素,FSH)与局部产生的调节分子之间的复杂相互作用介导。我们之前证明了可卡因和苯丙胺调节转录物(CART)的表达与卵泡健康状况呈负相关,并且CART在调节牛颗粒细胞基础雌二醇产生方面具有新的局部负向作用。然而,CART对FSH诱导的雌二醇产生的影响以及介导CART对颗粒细胞生理作用的潜在机制尚不清楚。本研究的目的是使用牛颗粒细胞原代培养物来确定CART对基础和FSH诱导的细胞内cAMP水平、芳香化酶mRNA、雌二醇积累、钙信号以及相关细胞内信号通路的影响。CART处理可有效抑制FSH诱导的颗粒细胞cAMP水平升高、雌二醇积累和芳香化酶mRNA。此外,结果表明钙对于FSH诱导的cAMP和雌二醇积累至关重要,并且CART显著抑制FSH诱导的钙内流。使用了选择性G蛋白和蛋白激酶抑制剂来阐明参与CART作用的途径。CART对FSH信号传导和雌二醇产生的抑制作用是通过G(o/i)依赖性途径介导的,而其他信号抑制剂对CART的作用均无影响。结果证明了CART对与雌二醇产生和卵泡发育相关的FSH信号通路多个组分具有新的强效抑制作用,并为CART在生殖系统内外潜在相关的作用机制提供了新的见解。